Lithium (Li) metal anodes are attractive for high-energy-density batteries. Dead Li is inevitably generated during the delithiation of deposited Li based on a conversion reaction, which severely depletes active Li and electrolyte and induces a short lifespan. In this contribution, a successive conversion-deintercalation (CTD) delithiation mechanism is proposed by manipulating the overpotential of the anode to restrain the generation of dead Li. The delithiation at initial cycles is solely carried out by a conversion reaction of Li metal. When the overpotential of the anode increases over the delithiation potential of lithiated graphite after cycling, a deintercalation reaction is consequently triggered to complete a whole CTD delithiation process, largely reducing the formation of dead Li due to a highly reversible deintercalation reaction. Under practical conditions, the working batteries based on a CTD delithiation mechanism maintain 210 cycles with a capacity retention of 80% in comparison to 110 cycles of a bare Li anode. Moreover, a 1 Ah pouch cell with a CTD delithiation mechanism operates for 150 cycles. The work ingeniously restrains the generation of dead Li by manipulating the delithiation mechanisms of the anode and contributes to a fresh concept for the design of practical composite Li anodes.
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http://dx.doi.org/10.1021/jacs.1c08606 | DOI Listing |
Adv Sci (Weinh)
December 2024
Institute of Materials Science, Technische Universität Darmstadt, Peter-Grünberg-Str. 2, D-64287, Darmstadt, Germany.
The design of cathode/electrolyte interfaces in high-energy density Li-ion batteries is critical to protect the surface against undesirable oxygen release from the cathodes when batteries are charged to high voltage. However, the involvement of the engineered interface in the cationic and anionic redox reactions associated with (de-)lithiation is often ignored, mostly due to the difficulty to separate these processes from chemical/catalytic reactions at the cathode/electrolyte interface. Here, a new electron energy band diagrams concept is developed that includes the examination of the electrochemical- and ionization- potentials evolution upon batteries cycling.
View Article and Find Full Text PDFAdv Mater
December 2024
Institute of Physical Chemistry, Justus Liebig University Giessen, Heinrich-Buff-Ring 17, D-35392, Giessen, Germany.
Silicon is a promising negative electrode material for solid-state batteries (SSBs) due to its high specific capacity and ability to prevent lithium dendrite formation. However, SSBs with silicon electrodes currently suffer from poor cycling stability, despite chemical engineering efforts. This study investigates the cycling failure mechanism of composite Si/LiPSCl electrodes by decoupling the effects of interface chemical degradation and mechanical cracking.
View Article and Find Full Text PDFACS Energy Lett
December 2024
School of Materials Science and Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.
Solid-state batteries (SSBs) with silicon anodes could enable improved safety and energy density compared to lithium-ion batteries. However, degradation arising from the massive volumetric changes of silicon anodes during cycling is not well understood in solid-state systems. Here, we use X-ray computed microtomography to reveal micro- to macro-scale chemo-mechanical degradation processes of silicon anodes in SSBs.
View Article and Find Full Text PDFSmall
December 2024
Department of Energy Science, Sungkyunkwan University, Suwon, 16419, Republic of Korea.
Uplifting the charging voltage of LiCoO is crucial for surpassing current energy density thresholds in Li-ion batteries. However, the structural and chemical instability of LiCoO in the deeply delithiated state is a major obstacle to the practical implementation of high-voltage LiCoO. This study proposes a multi-element co-doped LiCoO that exhibits enhanced electrochemical performances at 4.
View Article and Find Full Text PDFACS Nano
December 2024
Institute of Energy: Sustainability, Environment, and Equity, Stony Brook University, Stony Brook, New York 11794, United States.
Significant demand for lithium-ion batteries necessitates alternatives to Co- and Ni-based cathode materials. Cation-disordered materials using earth-abundant elements are being explored as promising candidates. In this paper, we demonstrate a coprecipitation synthetic approach that allows direct preparation of disordered rocksalt LiFeTiO (r-LFTO·C) and spinel structured hybrid LiFeTiO·C (s-LFTO·C) nanoparticles with a conformal conductive carbon coating.
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